esv3779623
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:inversion
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:291,307
- Description:Chr13:g.73200442_72909136inv
- Publication(s):Forbes et al. 2008, Forbes et al. 2008, Robinson et al. 2012
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 882 SVs from 70 studies. See in: genome view
Overlapping variant regions from other studies: 882 SVs from 70 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3779623 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 72,334,998 | 72,626,304 |
| esv3779623 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 72,909,136 | 73,200,442 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16605419 | inversion | 1732913 | Curated | Curated | 13 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16605419 | Remapped | Perfect | NC_000013.11:g.723 34998_72626304inv | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 72,334,998 | 72,626,304 |
| essv16605419 | Submitted genomic | NC_000013.10:g.729 09136_73200442inv | GRCh37 (hg19) | NC_000013.10 | Chr13 | 72,909,136 | 73,200,442 |